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Clinical Trials/NCT01449890
NCT01449890
Completed
N/A

Randomized Trial of E-mail Follow-up Care After Cognitive Behavioural Treatment for Depression

Universitätsklinikum Hamburg-Eppendorf1 site in 1 country92 target enrollmentSeptember 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Depressive Disorders
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Enrollment
92
Locations
1
Primary Endpoint
Measure of the severity of depression - Beck Depression Inventory (BDI- II)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The primary objective of this study is to test in a randomized effectiveness trial if e-mail delivered cognitive behavioural treatment is an effective follow-up care approach in the treatment of depression under clinically representative conditions.

Detailed Description

Depression belongs to the most prevalent mental disorders and often goes along with a high burden of disease. Although the efficacy and the effectiveness of psychological treatments for depressive disorders have been demonstrated, there remains the problem of maintaining the benefits achieved during the initial treatment phase. Therefore options of follow-up care have to be considered. Since access to psychotherapeutic treatments is limited and costly, internet-based interventions can offer a feasible opportunity for follow-up care in order to enhance the long-term effectiveness of psychotherapy.

Registry
clinicaltrials.gov
Start Date
September 2012
End Date
November 2013
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

PD Dr. phil. Birgit Watzke

Principal Investigator

Universitätsklinikum Hamburg-Eppendorf

Eligibility Criteria

Inclusion Criteria

  • Depressive disorder: F32.0-F32.2; F33.0-F33.2; F34.1 according to ICD-10
  • Precursory CBT
  • Internet access

Exclusion Criteria

  • No knowledge of the German language
  • Risk of suicide
  • Acute psychosis or psychotic symptoms
  • Established concurrent in vivo CBT after discharge from inpatient CBT

Outcomes

Primary Outcomes

Measure of the severity of depression - Beck Depression Inventory (BDI- II)

Time Frame: Change in the BDI-II from baseline (beginning of treatment) to follow up (3 months after termination of the follow-up care)

Secondary Outcomes

  • Depressive relapse/recurrence(Measured at follow up (3 months after termination of the follow-up care))
  • Measure of health related quality of life - SF-8(Change in the SF-8 from baseline (beginning of treatment) to follow up (3 months after termination of the follow-up care)
  • GAD-7(Change in the GAD-7 from baseline (beginning of treatment) to follow up (3 months after termination of the follow-up care))

Study Sites (1)

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